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The Biochemical Journal
|
October 1, 1983
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liver
G H Elder, J A Tovey, D M Sheppard
Clinical Psychology Review
|
September 1, 1999
Tourette's and comorbid syndromes: obsessive compulsive and attention deficit hyperactivity disorder. A common etiology?
D M Sheppard, J L Bradshaw, R Purcell, et al.
Journal of Cancer Survivorship : Research and Practice
|
November 13, 2019
Building a novel occupational rehabilitation program to support cancer survivors to return to health, wellness, and work in Australia
D M Sheppard, D Frost, M Jefford, et al.
Human Genetics
|
January 1, 1982
Tetraploid conceptus with three paternal contributions
D M Sheppard, R A Fisher, S D Lawler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 14, 1999
Effects of stimulant medication on the lateralisation of line bisection judgements of children with attention deficit hyperactivity disorder
D M Sheppard, J L Bradshaw, J B Mattingley, et al.
Clinical Science (London, England : 1979)
|
June 1, 1980
Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase
G H Elder, D M Sheppard, R E De Salamanca, et al.
Lancet (London, England)
|
June 11, 1983
Immunoreactive uroporphyrinogen decarboxylase in porphyria cutanea tarda
G H Elder, D M Sheppard, J A Tovey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
Movement sequencing in children with Tourette's syndrome and attention deficit hyperactivity disorder
D M Sheppard, J L Bradshaw, N Georgiou, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1987
Cytogenetic analysis of four human ovarian carcinoma cell lines
D Sheer, D M Sheppard, P A Gorman, et al.
Annals of Human Genetics
|
July 1, 1985
Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17
D Sheer, D M Sheppard, M le Beau, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
The Biochemical Journal
|
October 1, 1983
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liver
G H Elder, J A Tovey, D M Sheppard
Clinical Psychology Review
|
September 1, 1999
Tourette's and comorbid syndromes: obsessive compulsive and attention deficit hyperactivity disorder. A common etiology?
D M Sheppard, J L Bradshaw, R Purcell, et al.
Journal of Cancer Survivorship : Research and Practice
|
November 13, 2019
Building a novel occupational rehabilitation program to support cancer survivors to return to health, wellness, and work in Australia
D M Sheppard, D Frost, M Jefford, et al.
Human Genetics
|
January 1, 1982
Tetraploid conceptus with three paternal contributions
D M Sheppard, R A Fisher, S D Lawler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 14, 1999
Effects of stimulant medication on the lateralisation of line bisection judgements of children with attention deficit hyperactivity disorder
D M Sheppard, J L Bradshaw, J B Mattingley, et al.
Clinical Science (London, England : 1979)
|
June 1, 1980
Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase
G H Elder, D M Sheppard, R E De Salamanca, et al.
Lancet (London, England)
|
June 11, 1983
Immunoreactive uroporphyrinogen decarboxylase in porphyria cutanea tarda
G H Elder, D M Sheppard, J A Tovey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
Movement sequencing in children with Tourette's syndrome and attention deficit hyperactivity disorder
D M Sheppard, J L Bradshaw, N Georgiou, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1987
Cytogenetic analysis of four human ovarian carcinoma cell lines
D Sheer, D M Sheppard, P A Gorman, et al.
Annals of Human Genetics
|
July 1, 1985
Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17
D Sheer, D M Sheppard, M le Beau, et al.
Page
of 3